chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	49904049	49904050	C	-	17	GENIC	homozygous	49755338
13	49908025	49908027	TG	--	35	GENIC	heterozygous	50580299
13	49928097	49928098	G	-	14	GENIC	heterozygous	50562924
13	49931071	49931072	C	CCTAAGAAATA	45	GENIC	heterozygous	50517564
13	49931074	49931075	C	CA	45	GENIC	heterozygous	50517565
13	49931075	49931076	T	TA	44	GENIC	heterozygous	50517566
13	49931080	49931081	T	TATG	47	GENIC	heterozygous	50517567
13	49931084	49931085	A	-	45	GENIC	heterozygous	50517568
13	49962473	49962474	G	T	5	GENIC	homozygous	49755344
13	49965350	49965351	T	TTGTGTGTGTGTGTGTG	14	GENIC	homozygous	50517569
13	49991865	49991866	A	AAAG	5	GENIC	homozygous	50580300
13	49995004	49995005	C	CTT	12	GENIC	heterozygous	50029340
13	49995989	49995990	A	-	12	GENIC	heterozygous	50191671
13	49999629	49999630	C	-	5	GENIC	homozygous	50517571
13	50000086	50000087	C	CT	3	GENIC	heterozygous	50517572
13	49962475	49962476	C	T	5	GENIC	homozygous	49755345
13	49996666	49996667	G	GGT	7	GENIC	heterozygous	49946988
13	50018322	50018323	T	A	23	GENIC	homozygous	49755351
13	50022190	50022191	T	TAC	9	GENIC	heterozygous	50517573
13	50022199	50022201	AC	--	9	GENIC	heterozygous	50517574
13	50023515	50023517	TT	--	10	GENIC	heterozygous	50029442